FDA Adverse Event Malfunction Summary report: N

FLOW-I C20

MDR report key: 8001204 · Received October 24, 2018

Report

Report Number
8010042-2018-00564
Event Type
Malfunction
Date Received
October 24, 2018
Report Date
November 26, 2018
Manufacturer
MAQUET CRITICAL CARE AB
Product Code
BSZ
PMA / PMN Number
K160665
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IT
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 0

GETINGE USA SALES, LLC (IMPORTER) IS SUBMITTING THIS REPORT ON BEHALF OF MAQUET CRITICAL CARE AB (MANUFACTURER). REF. EXEMPTION #: E2018003. GETINGE USA SALES, LLC 45 BARBOUR POND DRIVE WAYNE, NJ 07470. CONTACT PERSON: (B)(4).

Additional Manufacturer Narrative · 0

OUR COMPANY FIELD SERVICE ENGINEER (FSE) STATES THAT NO DEVIATIONS OR FAULTS COULD BE SEEN WHEN THE ANESTHESIA WORKSTATION WAS INVESTIGATED AT THE HOSPITAL. NO PARTS WERE REPLACED. THE UNIT WAS RETURNED TO CLINICAL USE. THE LOG CONTAINS ALARMS FOR HIGH PRESSURE BUT THE DATE OF THE ALLEGED EVENT IS NOT KNOWN. IT IS THEREFORE NOT POSSIBLE TO CONFIRM THE ALLEGED EVENT IN THE INTERNAL LOG. THERE ARE NO INDICATIONS OF ANY MALFUNCTIONS IN THE TECHNICAL LOG. WE HAVE NOT BEEN ABLE TO DETERMINE THE TRUE CASE OF THE REPORTED EVENT. GETINGE USA SALES, LLC (IMPORTER) IS SUBMITTING THIS REPORT ON BEHALF OF MAQUET CRITICAL CARE AB (MANUFACTURER). REF. EXEMPTION #: E2018003. GETINGE USA SALES, LLC 45 BARBOUR POND DRIVE WAYNE, NJ 07470. CONTACT PERSON: (B)(4).

Description of Event or Problem · 0

IT WAS REPORTED THAT DURING PATIENT TREATMENT, ALARMS FOR HIGH AIRWAY PRESSURE WERE GENERATED. THERE WAS NO PATIENT HARM. (B)(4).

Description of Event or Problem · 0

(B)(4).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
843290 FLOW-I C20 GAS-MACHINE, ANESTHESIA BSZ MAQUET CRITICAL CARE AB C20

Patients

Seq Age Sex Outcome Treatment
1